毛皮
突变
生物
冠状病毒
劈理(地质)
三角洲
Spike(软件开发)
遗传学
病毒学
分子生物学
基因
2019年冠状病毒病(COVID-19)
医学
生物化学
疾病
传染病(医学专业)
内科学
古生物学
经济
航空航天工程
酶
管理
工程类
断裂(地质)
作者
Yang Liu,Jianying Liu,Bryan A. Johnson,Hongjie Xia,Zhiqiang Ku,Craig Schindewolf,Steven G. Widen,Zhiqiang An,Scott C. Weaver,Vineet D. Menachery,Xuping Xie,Pei‐Yong Shi
出处
期刊:Cell Reports
[Elsevier]
日期:2022-04-29
卷期号:39 (7): 110829-110829
被引量:322
标识
DOI:10.1016/j.celrep.2022.110829
摘要
We report that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta spike mutation P681R plays a key role in the Alpha-to-Delta variant replacement during the coronavirus disease 2019 (COVID-19) pandemic. Delta SARS-CoV-2 efficiently outcompetes the Alpha variant in human lung epithelial cells and primary human airway tissues. The Delta spike mutation P681R is located at a furin cleavage site that separates the spike 1 (S1) and S2 subunits. Reverting the P681R mutation to wild-type P681 significantly reduces the replication of the Delta variant to a level lower than the Alpha variant. Mechanistically, the Delta P681R mutation enhances the cleavage of the full-length spike to S1 and S2, which could improve cell-surface-mediated virus entry. In contrast, the Alpha spike also has a mutation at the same amino acid (P681H), but the cleavage of the Alpha spike is reduced compared with the Delta spike. Our results suggest P681R as a key mutation in enhancing Delta-variant replication via increased S1/S2 cleavage.
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